Duns Number:008999906
Device Description: GuideLiner XL catheter is intended to be used in conjunction with a guide catheter to acce GuideLiner XL catheter is intended to be used in conjunction with a guide catheter to access discrete regions of the coronary and/or peripheral vasculature, and to facilitate placement of interventional devices.
Catalog Number
-
Brand Name
GuideLiner® XL catheter
Version/Model Number
5576
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
November 17, 2018
Issuing Agency
In HIBCC
MRI safety Status
Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)
-
Device labeled as "Not made with natural rubber latex"
-
For Single-Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
DQY
Product Code Name
Catheter, Percutaneous
Public Device Record Key
b372c2cf-5a19-4806-a96e-bfdb87e4374b
Public Version Date
December 22, 2021
Public Version Number
9
DI Record Publish Date
September 05, 2016
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 6 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 238 |
| U | Unclassified | 12 |